Scission of human apolipoprotein B-100 by kallikrein: characterization of the cleavage site

Biochem Biophys Res Commun. 1986 Jun 13;137(2):821-5. doi: 10.1016/0006-291x(86)91153-8.

Abstract

Low density lipoprotein (LDL) from human plasma was digested with the specific endoprotease, kallikrein. Apolipoprotein B-100, the protein moiety of LDL, was cleaved by kallikrein into two fragments (K1 and K2) which we have compared to the naturally occurring fragments, B-74 and B-26. We have found that K1 and K2 precisely match B-74 and B-26 with respect to molecular weight, stoichiometry, and amino terminal amino acid sequence. These findings provide strong evidence that kallikrein is the agent responsible for the formation of B-74 and B-26 in human LDL.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Apolipoprotein B-100
  • Apolipoproteins B / metabolism*
  • Binding Sites
  • Humans
  • Kallikreins / metabolism*
  • Peptide Fragments / analysis

Substances

  • Apolipoprotein B-100
  • Apolipoproteins B
  • Peptide Fragments
  • Kallikreins